Search results for "Styrene"

showing 10 items of 561 documents

Synthesis of 3D dendritic gold nanostructures assisted by a templated growth process: Application at the detection of traces of molecules

2020

International audience; Complex architectures like 3D gold dendritic nanostructures were synthesized by an in situ templated growth method using a thin film of a block copolymer [polystyrene-b-poly(4-vinylpyridine)] deposited onto silicon substrates. The overall study has demonstrated the strong link between the morphology, size, and distribution of the structures and the synthetic physicochemical parameters, such as pH, reaction temperature, concentration, and nature of reactants. A nonequilibirum state of the medium has been required to create a fractal growth of the gold structures onto a prepatterned gold-seeded surface and has led to a better control of the structures' surface coverage…

Materials scienceNanostructureSiliconchemistry.chemical_element02 engineering and technologySurfaces and Interfaces010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsElectrochemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundAdsorptionchemistryChemical engineeringElectrochemistryCopolymerMolecule[CHIM]Chemical SciencesGeneral Materials SciencePolystyreneThin film0210 nano-technologySpectroscopy
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Crystallization kinetics of colloidal binary mixtures with depletion attraction.

2014

In this work the crystallization kinetics of colloidal binary mixtures with attractive interaction potential (Asakura–Oosawa) has been addressed. Parameters such as fraction of crystals, linear crystal dimension and crystal packing have been quantified in order to understand how the crystal formation is driven in terms of the depth of the attractive potential and the composition of the binary mixture (described by the number ratio). It was found that inside the eutectic triangle, crystallization is mainly governed by nucleation and the crystal packing is close to the close-packing of hard spheres. Moving out from the eutectic triangle towards small component results in the crystallization o…

Materials scienceNucleationPhysics::OpticsGeneral ChemistryHard spheresCondensed Matter Physicslaw.inventionCondensed Matter::Soft Condensed MatterCrystalchemistry.chemical_compoundCrystallographyColloidchemistryChemical physicslawCondensed Matter::SuperconductivityStatic light scatteringPolystyreneCrystallizationEutectic systemSoft matter
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Advances in organic and organic-inorganic hybrid polymeric supports for catalytic applications

2016

In this review, the most recent advances (2014–2016) on the synthesis of new polymer-supported catalysts are reported, focusing the attention on the synthetic strategies developed for their preparation. The polymer-supported catalysts examined will be organic-based polymers and organic-inorganic hybrids and will include, among others, polystyrenes, poly-ionic liquids, chiral ionic polymers, dendrimers, carbon nanotubes, as well as silica and halloysite-based catalysts. Selected examples will show the synthesis and application in the field of organocatalysis and metal-based catalysis both for non-asymmetric and asymmetric transformations.

Materials sciencePharmaceutical ScienceAsymmetric catalysiHomogeneous catalysisNanotechnologyReviewCarbon nanotube010402 general chemistryHeterogeneous catalysis01 natural sciencesAnalytical ChemistryCatalysislaw.inventionlcsh:QD241-441Heterogeneous catalysiOrganocatalysilcsh:Organic chemistrylawDendrimerDrug DiscoveryOrganic-inorganic hybridOrganic chemistryorganocatalysisPhysical and Theoretical ChemistryPolystyrenechemistry.chemical_classification010405 organic chemistryMedicine (all)Organic ChemistryEnantioselective synthesisasymmetric catalysisPolymerAsymmetric catalysis; Heterogeneous catalysis; Metal catalyst; Organic-inorganic hybrid; Organocatalysis; Polystyrene; Medicine (all); Organic ChemistrySettore CHIM/06 - Chimica OrganicaMetal catalyst0104 chemical sciencesheterogeneous catalysischemistryChemistry (miscellaneous)OrganocatalysisMolecular Medicine
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Capacitive scanning dilatometry and frequency-dependent thermal expansion of polymer films

2000

The dilatometric properties of polymer films near and above their glass-transition temperatures were explored using capacitive high-frequency detection in temperature ramping as well as in harmonic temperature cycling experiments. The broad applicability of capacitive scanning dilatometry is demonstrated by the investigation of macromolecular systems of vastly different polarity such as polystyrene, polybutadiene, and polyvinylacetate. From temperature cycling experiments the real and imaginary parts of the frequency-dependent thermal-expansion coefficient are determined in the sub-Hz regime.

Materials sciencePolarity (physics)Capacitive sensingInstitut für Physik und AstronomieTemperature cycling530Thermal expansionchemistry.chemical_compoundPolybutadienechemistryThermomechanical analysisPolystyreneComposite materialGlass transitioninfo:eu-repo/classification/ddc/530Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics
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A contribution to the kinetics of the polymerization of styrene with CF3SO3H as catalyst

1978

The time dependence of the cationic polymerization of styrene in CH2Cl2 with CF3SO3H as catalyst can be formally described as being first-order with respect to monomer concentration [M]0. The reaction rate shows a third-order dependence in catalyst concentration [C]0. A high polymer and a low polymer polystyrene fraction are found at [M]0>0.2 mole · l−. The reaction rate of the high polymer fraction is proportional to [C] 0 3 , that of the low polymer fraction probably proportional to [C] 0 2 . The polymerization active species may thus be triple ions in the first and ion pairs in the second case.

Materials sciencePolymers and PlasticsCationic polymerizationSolution polymerizationGeneral ChemistryCondensed Matter PhysicsStyrenechemistry.chemical_compoundMonomerChain-growth polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryAddition polymerPolystyrenePolymer Bulletin
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Blends of poly(2,6-dimethyl-1,4-phenylene oxide) with styrene copolymers

1994

Binary blends of poly(2,6–dimethyl–1,4–phenylene oxide) (PPE) with various styrene copolymers were investigated. Poly(styrene–co–acrylonitrile) (SAN), poly[styrene–co–(methyl methacrylate)] (SMMA), poly[styrene–co–(acrylic acid)] (SAA) and poly[styrene–co–(maleic anhydride)] (SMA) are only miscible with PPE when the amount of comonomer is rather small. From calculated binary interaction densities it can be concluded that the strong repulsion between PPE and comonomer limits miscibility. In blends of PPE with SAN, as well as with ABS, the inter-facial tension between the blend components is significantly reduced upon addition of polystyrene–block–poly–(methyl methacrylate) diblock copolymers…

Materials sciencePolymers and PlasticsComonomerOrganic ChemistryMaleic anhydrideCondensed Matter PhysicsMiscibilityStyrenechemistry.chemical_compoundchemistryPhenylenePolymer chemistryMaterials ChemistryCopolymerMethyl methacrylateAcrylic acidMacromolecular Symposia
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Isoprene/Styrene Tapered Multiblock Copolymers with up to Ten Blocks: Synthesis, Phase Behavior, Order, and Mechanical Properties

2018

The living anionic copolymerization of isoprene and styrene in cyclohexane affords tapered block copolymers due to the highly disparate reactivity ratios of rI = 12.8 and rS = 0.051. Repeated addit...

Materials sciencePolymers and PlasticsCyclohexaneOrganic ChemistryMultiblock copolymerSynthesis Phase02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesStyreneInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCopolymerOrder (group theory)Reactivity (chemistry)0210 nano-technologyIsopreneMacromolecules
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The effect of THF and the chelating modifier DTHFP on the copolymerisation of β-myrcene and styrene: kinetics, microstructures, morphologies, and mec…

2022

The statistical anionic copolymerisation of the biobased monomer β-myrcene with styrene in cyclohexane was investigated via in situ near-infrared (NIR) spectroscopy, focusing on the influence of the modifiers (i.e., Lewis bases) tetrahydrofuran (THF) and 2,2-di(2-tetrahydrofuryl)propane (DTHFP) on the reactivity ratios. With increasing [modifier]/[Li] ratio, the reactivity ratios in the system myrcene/styrene are adjustable from rS ≪ rMyrvia rS ≈ rMyr to rS ≫ rMyr. The bidentate modifier DTHFP affects the reactivity ratios much more than THF: minute amounts only (0.35 equivalent relative to Li) are required to randomize the copolymer, and one equivalent to invert the reactivity ratios. Usin…

Materials sciencePolymers and PlasticsCyclohexaneSmall-angle X-ray scatteringOrganic ChemistryBioengineering02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology54001 natural sciencesBiochemistry0104 chemical sciencesStyrenechemistry.chemical_compoundchemistryCopolymerPhysical chemistryLamellar structureReactivity (chemistry)0210 nano-technologyGlass transitionTetrahydrofuran
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Pressure dependence of the demixing of polymer solutions determined by viscometry

1981

From the break-down in the viscosity of a polymer solution, associated with the entrance into the two phase region, the pressure dependence of the demixing temperatures of solutions of polystyrene (M = 600.000) in cyclohexane, cyclopentane, diethylmalonate and 1-phenyldecane was measured up to 1000 bar. The application of pressure increases the solubility of polystyrene in cyclopentane and diethylmalonate, but decreases that in 1-phenyldecane; in the case of cyclohexane, a pressure of optimum miscibility is observed at ca. 120 bar.

Materials sciencePolymers and PlasticsCyclohexaneViscometerThermodynamicsMiscibilityHildebrand solubility parameterchemistry.chemical_compoundColloid and Surface ChemistrychemistryPhase (matter)Polymer chemistryMaterials ChemistryPolystyrenePhysical and Theoretical ChemistryCyclopentaneBar (unit)Colloid and Polymer Science
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Testing of a kinetics equation of mechanical degradation

1987

A modification of the kinetics equation of mechanical degradation of Harrington and Zimm is proposed to fit experimental data taken on a molten polystyrene. This equation is applied to each molecular weight of the discretized molecular weight distribution curve, and the limiting molecular weight is determined for each molecular weight. With this modification the theoretical curves fit both Mw and Mn curves well.

Materials sciencePolymers and PlasticsDiscretizationKineticsThermodynamicsGeneral ChemistryLimitingchemistry.chemical_compoundchemistryKinetic equationsKinetics equationMaterials ChemistryMolar mass distributionDegradation (geology)Physical chemistryPolystyrenePolymer Engineering and Science
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